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Orthostatic Tolerance in Mamma Cancer Patients After Anaesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00824876
Enrollment
Unknown
Registered
2009-01-19
Start date
2009-01-31
Completion date
Unknown
Last updated
2009-07-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Mammae cancer patients

Brief summary

The investigators want to investigate the effect of anaesthesia, on the ability to maintain upright posture immediately after surgery in mamma cancer patients. The investigators hypothesis is, that a standard anaesthesia does not effect the ability to maintain upright posture right after surgery.

Detailed description

It is known, that patients undergoing major surgery have problems maintaining upright posture after major surgery. This can be due to fall in bloodpressure, with symptoms like dizziness, nausea/vomiting and fainting. With this investigation, we want to prove that anaesthesia is not the decisive factor, in patients ability to maintain upright posture after surgery.

Interventions

None listed

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Months to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients having performed elective breast surgery * Age between 18 and 70 years * Patients who have given written consent to participate in the project after haven completely understood the contents and limitations of the protocol

Exclusion criteria

* Patients who do not understand or speak Danish * Patients who have not signed the informed consent or the written authority pre-medication, except 1g paracetamol * ASA \> II * Pregnant or breastfeeding * Known to have Renal disease * Known to have Psychiatric disorder (not considering the use of SSRI antidepressive) * Need for crash induction or prone position * Oesophageal varicoses * Necrosis or cancer in: Mouth, Pharynx, Larynx or Oesophagus * Coarctation or aneurism in the proximal Aorta * Severe bleeding disease

Design outcomes

Primary

MeasureTime frame
To investigate orthostatic function, measured by Finapress

Secondary

MeasureTime frame
To investigate the occurrence of postsurgery nausea/vomiting

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026